New CA Global AO Wave Sanitizer Gel 75

Manufacturer: C & A MARKETING, INC.
Effective date: 2021-02-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:37:45

Label at a glance#

ProductWave Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

■ Hand Sanirtizer to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

■ Dispense into dry hands and rub until dry. ■ Children under 6 years of age should be supervised by an adult when using this product.

Storage and handling

■ Store below 110ºF (43ºC) ■ May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ Hand Sanirtizer to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes, and if eye contact occurs, flush thoroughly with water and seek medical advice

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness occur.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Dispense into dry hands and rub until dry. ■ Children under 6 years of age should be supervised by an adult when using this product.

Other information

STORAGE AND HANDLING SECTION

■ Store below 110ºF (43ºC) ■ May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Polyacrylic acid, Trolamine, Water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	2
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	2
1305100	ethanol 75 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78754-003-02	2022-07-29	C162847	48780-1	e4f33bdf-a3c7-d8a0-e053-dadaa90a6e4e	New CA Global AO Wave Sanitizer Gel 75

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78754-003-02	Wave Hand Sanitizer	60 mL in 1 BOTTLE, PLASTIC	GEL	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78754-003	WAVE HAND SANITIZER (ALCOHOL) GEL [C & A MARKETING, INC.]	2	Legacy NDC, 1 package rows	20210204_b9e977ba-abae-60bc-e053-2995a90ac461.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Wave Hand Sanitizer
ALCOHOL
TROLAMINE
POLYACRYLIC ACID (250000 MW)
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78754-003	78754-003-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TROLAMINE	9O3K93S3TK	IACT
POLYACRYLIC ACID (250000 MW)	9G2MAD7J6W	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ba6666b1-74c1-1632-e053-2a95a90aeacf			b9e977ba-abae-60bc-e053-2995a90ac461	2021-02-02	Warnings	Exact identifier spl id: ba6666b1-74c1-1632-e053-2a95a90aeacf spl set id: b9e977ba-abae-60bc-e053-2995a90ac461

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.